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MALARIA CONSORTIUM UGANDARequest for proposal (RFP) for SUPPORT TO RESEARCH ACTIVITIES ON THE SEASONAL MALARIA CHEMOPREVENTION (SMC) RAPID ASSESSMENT IN THE DEMOCRATIC REPUBLIC OF CONGO (DRC)SPECIFICATIONS
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A non-randomized controlled trial is a type of clinical study where participants are assigned to different groups based on non-random criteria, often to compare the effects of a treatment or intervention against a control group.
Researchers and organizations conducting non-randomized controlled trials are required to file their studies, particularly if they involve significant interventions on human subjects or are intended for regulatory approval.
To fill out a non-randomized controlled trial, researchers typically need to provide a study protocol, participant information, consent forms, and data collection methods, ensuring all ethical guidelines are followed.
The purpose of a non-randomized controlled trial is to evaluate the effectiveness or safety of an intervention by comparing outcomes in a treatment group with those in a control group, without random assignment.
Key information that must be reported includes the trial objectives, methodology, participant demographics, results, and any adverse effects experienced during the study.
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